GB1119033A - Polymerization process and catalyst - Google Patents
Polymerization process and catalystInfo
- Publication number
- GB1119033A GB1119033A GB6392/66A GB639266A GB1119033A GB 1119033 A GB1119033 A GB 1119033A GB 6392/66 A GB6392/66 A GB 6392/66A GB 639266 A GB639266 A GB 639266A GB 1119033 A GB1119033 A GB 1119033A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- triethyl
- tribenzyl
- catalyst
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000003054 catalyst Substances 0.000 title abstract 3
- 238000006116 polymerization reaction Methods 0.000 title abstract 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- 229910052782 aluminium Inorganic materials 0.000 abstract 2
- 239000004411 aluminium Substances 0.000 abstract 2
- -1 aluminium halide Chemical class 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002902 organometallic compounds Chemical class 0.000 abstract 2
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- 229910010062 TiCl3 Inorganic materials 0.000 abstract 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052790 beryllium Inorganic materials 0.000 abstract 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 abstract 1
- 229910000072 bismuth hydride Inorganic materials 0.000 abstract 1
- BPBOBPIKWGUSQG-UHFFFAOYSA-N bismuthane Chemical compound [BiH3] BPBOBPIKWGUSQG-UHFFFAOYSA-N 0.000 abstract 1
- 229910052793 cadmium Inorganic materials 0.000 abstract 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 229910052733 gallium Inorganic materials 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052738 indium Inorganic materials 0.000 abstract 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 abstract 1
- 229910052744 lithium Inorganic materials 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 239000011777 magnesium Substances 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- MXHTZQSKTCCMFG-UHFFFAOYSA-N n,n-dibenzyl-1-phenylmethanamine Chemical group C=1C=CC=CC=1CN(CC=1C=CC=CC=1)CC1=CC=CC=C1 MXHTZQSKTCCMFG-UHFFFAOYSA-N 0.000 abstract 1
- FRQONEWDWWHIPM-UHFFFAOYSA-N n,n-dicyclohexylcyclohexanamine Chemical compound C1CCCCC1N(C1CCCCC1)C1CCCCC1 FRQONEWDWWHIPM-UHFFFAOYSA-N 0.000 abstract 1
- 150000002894 organic compounds Chemical class 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 239000002685 polymerization catalyst Substances 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 229910052701 rubidium Inorganic materials 0.000 abstract 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 229910052712 strontium Inorganic materials 0.000 abstract 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 abstract 1
- 229910052716 thallium Inorganic materials 0.000 abstract 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 abstract 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 abstract 1
- IFXORIIYQORRMJ-UHFFFAOYSA-N tribenzylphosphane Chemical compound C=1C=CC=CC=1CP(CC=1C=CC=CC=1)CC1=CC=CC=C1 IFXORIIYQORRMJ-UHFFFAOYSA-N 0.000 abstract 1
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical group C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 abstract 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical group CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Abstract
A polymerization catalyst composition is formed by mixing (a) a preformed complex of an aluminium halide of the formula AlX3 and an organo-compound of the formula R3M, (b) TiCl3, 1/3 AlCl3, and (c) an organometallic compound of the formula RyM1Xz, where R is a hydrocarbon radical, M is an element from Group V(a) of the Mendeleeff Periodic Table, M1 is a metal from Group I(A), II(A), or III(A), X is halogen, y is an integer of 1, 2 or 3, z is 0 or 1 or 2, and the sum of y+z is equal to the valency of M1. Compounds of formula R3M may be triethyl, ethyl di-tert.-butyl, tricyclohexyl, triphenyl, tritolyl, or tribenzyl phosphine, triethyl, tribenzyl, triphenyl, or tricyclohexylamine, triethyl, tributyl, or tribenzyl stilbine or bismuthine. Compound (c) is selected from organometallic compounds of zinc, cadmium, aluminium, gallium, magnesium, sodium, potassium, lithium, rubidium, beryllium, indium, thallium, and strontium. The catalyst is used to polymerize aliphatic olefins having up to 8 carbon atoms, using conventional "low-pressure" techniques. The polymerization may be effected in bulk, or in a hydrocarbon solvent. Hydrogen may be present, and the catalyst premixed. The exemplified monomer is propylene.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US43285765A | 1965-02-15 | 1965-02-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1119033A true GB1119033A (en) | 1968-07-03 |
Family
ID=23717870
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6392/66A Expired GB1119033A (en) | 1965-02-15 | 1966-02-14 | Polymerization process and catalyst |
Country Status (7)
Country | Link |
---|---|
US (1) | US3514434A (en) |
BE (1) | BE676416A (en) |
DE (1) | DE1645096A1 (en) |
ES (1) | ES321943A1 (en) |
FR (1) | FR1464374A (en) |
GB (1) | GB1119033A (en) |
NL (2) | NL6601919A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4135045A (en) * | 1970-10-02 | 1979-01-16 | Mitsui Petrochemical Industries, Ltd. | Process for polymerization of olefins and catalyst composition therefor |
JPS4932195B1 (en) * | 1970-10-02 | 1974-08-28 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL246112A (en) * | 1958-01-27 | Eastman Kodak Co | ||
GB888709A (en) * | 1959-07-17 | 1962-01-31 | Exxon Research Engineering Co | Cocrystallized vanadium-titanium catalyst components |
BE631995A (en) * | 1962-05-07 | |||
US3269996A (en) * | 1962-09-18 | 1966-08-30 | Exxon Research Engineering Co | Three-component polymerization catalysts containing coordination complexes |
US3367927A (en) * | 1963-05-24 | 1968-02-06 | Grace W R & Co | Polymerization process |
-
0
- NL NL133099D patent/NL133099C/xx active
-
1965
- 1965-02-15 US US432857A patent/US3514434A/en not_active Expired - Lifetime
-
1966
- 1966-01-14 DE DE19661645096 patent/DE1645096A1/en active Pending
- 1966-01-15 FR FR46042A patent/FR1464374A/en not_active Expired
- 1966-01-19 ES ES0321943A patent/ES321943A1/en not_active Expired
- 1966-02-14 BE BE676416D patent/BE676416A/xx unknown
- 1966-02-14 GB GB6392/66A patent/GB1119033A/en not_active Expired
- 1966-02-15 NL NL6601919A patent/NL6601919A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
DE1645096A1 (en) | 1970-06-04 |
FR1464374A (en) | 1966-12-30 |
US3514434A (en) | 1970-05-26 |
ES321943A1 (en) | 1966-12-16 |
NL6601919A (en) | 1966-08-16 |
BE676416A (en) | 1966-08-16 |
NL133099C (en) |
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